Social Media Indoor Tanning Study

December 2, 2021 updated by: Sherry Pagoto, University of Connecticut

Using a Narrative-Based Approach to Reducing Indoor Tanning

The purpose of this research is to develop a social media delivered intervention to reduce unprotected sun exposure in young adults with a history of tanning.

Study Overview

Detailed Description

We will use social marketing theory and a user-centered design approach to develop a social media intervention that engages young adults with a history of tanning to practice sun safety behaviors. We will incentivize young adults who have a history of tanning to create social media posts that encourage their peers to engage in sun safety. Focus groups of tanners guided the development of the intervention. Investigators will conduct a pilot feasibility trial where participants will be randomized to a condition in which they are incentivized to create sun safety social media messages to be posted on a sun safety social media account or a condition in which they are incentivized to create social media messages about how to use technology to support healthy lifestyle behaviors to be posted on a health technology social media account. The intervention will last 4 weeks. Feasibility outcomes include recruitment, retention, acceptability, participation, social media message engagement (likes, comments, shares), persuasive impact of messages, unprotected sun exposure, sun protection, and tanning behavior. This work will inform a fully powered randomized trial testing the efficacy of this intervention.

Study Type

Interventional

Enrollment (Actual)

66

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Connecticut
      • Storrs, Connecticut, United States, 06269
        • University of Connecticut

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 30 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Ages 18-30
  • Tanned indoors or outdoors at least once in the past year
  • Intends to tan indoors or outdoors this summer
  • Daily user of any social media platform

Exclusion Criteria:

  • No smartphone
  • Does not use a social media platform daily
  • Lives in a state with an average temperature <75 degrees in May
  • Inability to provide consent due to mental illness or a cognitive impairment
  • Non-English speaking
  • Prisoner

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Sun Safety Social Media Challenge
During this 4-week intervention, participants will be incentivized to create sun safety social media messages that will be distributed on our sun safety Twitter and Facebook feeds.
Participants will attend a webinar to learn how to create effective social media posts about sun safety and be oriented to the social media accounts on which the messages will be posted. They will be informed that posts should include a sun safety message (e.g., promoting sunscreen use and protective clothing/hats or discouraging risk behaviors like tanning and burning). They will be encouraged to be creative so that the message gets likes and shares. Participants will be encouraged to follow the feeds to see the engagement on their posts, to share the posts in their feed, and to see other participants' posts. Participants will receive a $10 Amazon gift card per post for a maximum of 6 posts ($60). The participant who created the post that receives the most likes, comments, and shares each week will win a $50 Amazon gift card.
Active Comparator: Digital Health Social Media Challenge
During this 4-week intervention, participants will be incentivized to create posts that promote the use of technology to engage in healthy lifestyle behaviors (diet, exercise) on our digital health Twitter and Facebook feeds.
Participants will attend a webinar to learn how to create effective social media posts about using technology to get healthy and be oriented to the social media accounts on which the messages will be posted. They will be informed that posts should mention some way that technology (e.g., mobile apps, wearables) can be used to promote a healthy habit (e.g., diet, exercise). They will be encouraged to be creative so that the message gets likes and shares. Participants will be encouraged to follow the feeds to see the engagement on their posts, to share the posts in their feed, and to see other participants' posts. Participants will receive a $10 Amazon gift card per post for a maximum of 6 posts ($60). The participant who created the post that receives the most likes, comments, and shares each week will win a $50 Amazon gift card.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Recruitment
Time Frame: Baseline
The number of completed respondents to recruitment ads, number of respondents eligible at initial screening, and number of respondents who completed baseline.
Baseline
Retention
Time Frame: 4-week follow-up
The % of participants in each condition who complete the follow-up assessment.
4-week follow-up
Acceptability
Time Frame: 4-week follow-up
Number of participants who selected agree or strongly agree on 5-point Likert scale rating of how likely participants would be to recommend the intervention to a friend, and how likely they would be to participate again.
4-week follow-up
Participation
Time Frame: 4-week follow-up
The number of posts created by participants
4-week follow-up
Post Engagement
Time Frame: 4 weeks
The median number of likes, shares and retweets, and unique commenters each participant post received.
4 weeks
Desirability of Tanning
Time Frame: Baseline
Scale measuring participants' belief that a tan is attractive. Scale ranges from 0-12 with higher scores indicating higher levels of belief that a tan is attractive.
Baseline
Desirability of Tanning
Time Frame: 4-week follow-up
Scale measuring participants' belief that a tan is attractive. Scale ranges from 0-12 with higher scores indicating higher levels of belief that a tan is attractive.
4-week follow-up
Desirability of Tanning Alternatives
Time Frame: Baseline
Average score on items relating to tanning alternative desirability. Scale ranges from 1 to 5, with higher scores indicating more positive attitudes towards tanning alternatives.
Baseline
Desirability of Tanning Alternatives
Time Frame: 4-week follow-up
Average score on items relating to tanning alternative desirability. Scale ranges from 1 to 5, with higher scores indicating more positive attitudes towards tanning alternatives.
4-week follow-up
Persuasive Impact of Participant Messages
Time Frame: 4-week follow-up
The mean of participants ratings for how persuasive they found each post (other than those they created) on a scale of 0-100, with higher scores indicating more persuasive.
4-week follow-up
Contamination
Time Frame: 4-week follow-up
The number of participants who report they saw the opposite conditions Facebook or Twitter feeds.
4-week follow-up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Outdoor Tanning Intentions
Time Frame: Baseline
Three items assessed intentions to tan even once, intentions to tan regularly in the next year, and intentions to quit on a 7-point scale (0=definitely will not, 6=definitely will).
Baseline
Outdoor Tanning Intentions
Time Frame: 4-week follow-up
Three items assessed intentions to tan even once, intentions to tan regularly in the next year, and intentions to quit on a 7-point scale (0=definitely will not, 6=definitely will).
4-week follow-up
Sun Exposure
Time Frame: Baseline
How many hours the participant spent outside per week between the hours of 10am and 4pm.
Baseline
Sun Exposure
Time Frame: 4-week follow-up
How many hours the participant spent outside per week between 10am and 4pm
4-week follow-up
Outdoor Tanning
Time Frame: Baseline
How many times in the last 4 weeks the participant went outside for the purpose of tanning in the sun.
Baseline
Outdoor Tanning
Time Frame: 4-week follow-up
How many times in the last 4 weeks the participant went outside for the purpose of tanning in the sun.
4-week follow-up
Sun Protection
Time Frame: Baseline
Number of participants who reported using sun protection (sunscreen, protective clothing) often or always in the past month
Baseline
Sun Protection
Time Frame: 4-week follow-up
Number of participants who reported using sun protection (sunscreen, protective clothing) often or always in the past month
4-week follow-up
Indoor Tanning Behavior
Time Frame: Baseline
Number of indoor tanning visits in the previous month
Baseline
Indoor Tanning Behavior
Time Frame: 4 weeks
Number of indoor tanning visits in the previous month
4 weeks
Sunburn
Time Frame: baseline
Number of participants with 1 or more sunburns in the past month
baseline
Sunburn
Time Frame: 4 weeks
Number of participants with 1 or more sunburns in the past month
4 weeks
Outdoor Tanning Duration
Time Frame: 4 weeks
Median reported average number of minutes tanned per episode in the past 4 weeks, among participants who tanned in the past 4 weeks.
4 weeks
Outdoor Tanning Duration
Time Frame: Baseline
Median reported average number of minutes tanned per episode in the past 4 weeks, among participants who tanned in the past 4 weeks.
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sherry L Pagoto, PhD, University of Connecticut

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 6, 2020

Primary Completion (Actual)

October 28, 2020

Study Completion (Actual)

October 28, 2020

Study Registration Dates

First Submitted

February 7, 2019

First Submitted That Met QC Criteria

February 7, 2019

First Posted (Actual)

February 8, 2019

Study Record Updates

Last Update Posted (Actual)

January 3, 2022

Last Update Submitted That Met QC Criteria

December 2, 2021

Last Verified

December 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • H19-033
  • R21CA226133-01 (U.S. NIH Grant/Contract)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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